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临床试验/NCT05193318
NCT05193318终止2 期

Ketamine-assisted Psychotherapy for the Treatment of Persistent Depression in Abstinent Opioid Users

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2022年1月13日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
终止
入组人数
5
试验地点
1
主要终点
Montgomery Asberg Depression Rating Scale

研究概览

简要总结

The purpose of the study is to examine whether an investigational medication called ketamine along with psychotherapy is an effective treatment for depression in participants with a history of opioid addiction who have not abused opioids in at least 3 months. Participants will receive ketamine through intramuscular injection along with psychotherapy weekly for 8 weeks. Participation for eligible subjects who decide to enroll (including post-medication follow-up visits) will last about 16 weeks or 4 months.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Ketamine-assisted psychotherapy

Experimental

Subjects will receive 8 weekly intramuscular injections of ketamine hydrochloride starting at 0.5 mg/kg and increasing to a maximum dose of 1.5 mg/kg or a total dose of 60 mg, whichever is lower. Ketamine administration will be accompanied by psychotherapy before, after and during the session.

干预措施: Ketamine-assisted psychotherapy (Drug)

结局指标

主要结局

Montgomery Asberg Depression Rating Scale

时间窗: Change from baseline measured at week 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, and 16

Montgomery Asberg Depression Rating Scale (MADRS). The MADRS is a clinician administered, 10-item questionnaire of depression severity. The total score ranges from 0-60, with scores of 0-6 considered normal (non-depressed), 7-19 indicative of mild depression, 20-34 indicative of moderate depression, and 35-60 indicative of severe depression. Individuals scoring 20 or higher on the MADRS will be included in the study. The MADRS evaluates the following symptoms of depression: 1) clinical appearance of sadness, 2) self-reported sadness, 3) inner tension, 4) reduced sleep, 5) reduced appetite, 6) concentration difficulties, 7) lassitude, 8) inability to feel, 9) pessimistic thought process, and 10) thoughts of suicide. Lower scores are better (less depression).

次要结局

  • Beck Depression Inventory(Change from baseline measured at week 1-9, 10, 12, and 16)
  • Visual Analog Scale (VAS)(Change relative to baseline measured at week 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, and 16)
  • Generalized Anxiety Disorder-7 (GAD-7)(Change in score relative to baseline calculated at week 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, and 16.)
  • Mystical Experience Questionnaire (MEQ)(Measured at week 1-8)
  • Brief Pain Inventory (BPI)(Measured at baseline, week 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, and 16)
  • PTSD Checklist (PCL-5; PTSD Checklist 5)(Measured at week 1-9, 10, 12, and 16)
  • Timeline Follow-back (TLFB)(Measured at week 1-9, 10, 12, and 16)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Eric Dobson

Principal Investigator

Medical University of South Carolina

研究点 (1)

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